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临床试验/NCT03610906
NCT03610906Enrolling By Invitation不适用

Advancing Treatment for Pediatric Craniopharyngioma: Prospective Pilot Study Identifying Clinically Relevant Biological Targets for Medical Therapy

University of Colorado, Denver1 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2019年3月12日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
250
试验地点
1
主要终点
Identification of Potential Therapeutic Targets

研究概览

简要总结

New data suggests that the current treatment for pediatric adamantinomatous craniopharyngioma (CPA) may not be as effective as it could be.

详细描述

Current treatment regimens for pediatric CPA are limited to surgery and radiation therapy. This pilot study seeks to identify biologically rational therapeutics for the medical treatment of adamantinomatous CPA by confirming the overexpression of specific molecules.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
30 Days 至 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients between 0-21 years of age.
  • Patients with the diagnosis or clinical suspicion of craniopharyngioma in whom planned clinical management will include tissue sampling.

排除标准

  • Patients in whom final pathology does not demonstrate adamantinomatous craniopharyngioma
  • Patients in whom tissue specimen is not obtained/available
  • Patients over 21 years of age.
  • Patients who choose not to participate

结局指标

主要结局

Identification of Potential Therapeutic Targets

时间窗: Beginning of study to end of study, up to 1 year.

Investigators will identify potential therapeutic targets through mRNA expression.

次要结局

  • Progression Free Survival (PFS)(Beginning of study up to age 21 or death, whichever comes first.)
  • Visual Deficit Assessment(At 6 and 12 months after the specimen sample was taken.)
  • Pituitary Function Assessment(At 6 and 12 months after the specimen sample was taken.)
  • Survival(Beginning of study up to age 21 or death, whichever comes first.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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